Cryderman D E, Tang H, Bell C, Gilmour D S, Wallrath L L
Department of Biochemistry, 4-772 Bowen Science Building, University of Iowa, Iowa City, IA 52242, USA.
Nucleic Acids Res. 1999 Aug 15;27(16):3364-70. doi: 10.1093/nar/27.16.3364.
In a variety of organisms, genes placed near heterochromatin are transcriptionally silenced. In order to understand the molecular mechanisms responsible for this block in transcription, high resolution in vivo chromatin structure analysis was performed on two heat shock genes, hsp26 and hsp70. These genes normally reside in euchromatin where GAGA factor and RNA Pol II are present on the promoter prior to heat shock induction. P-element transformation experiments led to the identification of stocks in which these two genes were inserted within heterochromatin of the chromosome 4 telomeric region. These transgenes exhibit silencing that is partially suppressed by mutations in the gene encoding HP1. Micrococcal nuclease analysis revealed that the heterochromatic transgenes were packaged in a more regular nucleosome array than when located in euchromatin. High resolution DNase I analysis demonstrated that GAGA factor and TFIID were not associated with these promoters in heterochromatin; potassium permanganate experiments showed a loss of Pol II association. Taken together, these data suggest that occlusion of trans-acting factors from their cis- acting regulatory elements leading to a block in promoter potentiation is a mechanism for heterochromatin gene silencing.
在多种生物体中,位于异染色质附近的基因会发生转录沉默。为了理解导致转录受阻的分子机制,对两个热休克基因hsp26和hsp70进行了高分辨率的体内染色质结构分析。这些基因通常位于常染色质中,在热休克诱导之前,启动子上存在GAGA因子和RNA聚合酶II。P因子转化实验导致鉴定出一些品系,其中这两个基因插入到4号染色体端粒区域的异染色质内。这些转基因表现出沉默,编码HP1的基因突变可部分抑制这种沉默。微球菌核酸酶分析表明,异染色质转基因比位于常染色质时包装在更规则的核小体阵列中。高分辨率DNase I分析表明,GAGA因子和TFIID在异染色质中不与这些启动子结合;高锰酸钾实验显示Pol II结合丧失。综合这些数据表明,反式作用因子与其顺式作用调控元件的隔离导致启动子增强受阻,这是异染色质基因沉默的一种机制。